Li M - Search Results

1

Uncovering the total heritability explained by all true susceptibility variants in a genome-wide association study.

So HC, Li M, Sham PC. So HC, et al. Among authors: li m. Genet Epidemiol. 2011 Sep;35(6):447-56. doi: 10.1002/gepi.20593. Epub 2011 May 26. Genet Epidemiol. 2011. PMID: 21618601

2

Power of transmission/disequilibrium tests in admixed populations.

Li MX, Jiang L, Song YQ, Sham PC. Li MX, et al. Genet Epidemiol. 2008 Jul;32(5):434-44. doi: 10.1002/gepi.20316. Genet Epidemiol. 2008. PMID: 18278814

3

A knowledge-based weighting framework to boost the power of genome-wide association studies.

Li MX, Sham PC, Cherny SS, Song YQ. Li MX, et al. PLoS One. 2010 Dec 31;5(12):e14480. doi: 10.1371/journal.pone.0014480. PLoS One. 2010. PMID: 21217833 Free PMC article.

4

Identification of genes with allelic imbalance on 6p associated with nasopharyngeal carcinoma in southern Chinese.

Li Y, Fu L, Wong AM, Fan YH, Li MX, Bei JX, Jia WH, Zeng YX, Chan D, Cheung KM, Sham P, Chua D, Guan XY, Song YQ. Li Y, et al. Among authors: li mx. PLoS One. 2011 Jan 20;6(1):e14562. doi: 10.1371/journal.pone.0014562. PLoS One. 2011. PMID: 21283797 Free PMC article.

5

GATES: a rapid and powerful gene-based association test using extended Simes procedure.

Li MX, Gui HS, Kwan JS, Sham PC. Li MX, et al. Am J Hum Genet. 2011 Mar 11;88(3):283-93. doi: 10.1016/j.ajhg.2011.01.019. Am J Hum Genet. 2011. PMID: 21397060 Free PMC article.

6

Comparisons of seven algorithms for pathway analysis using the WTCCC Crohn's Disease dataset.

Gui H, Li M, Sham PC, Cherny SS. Gui H, et al. Among authors: li m. BMC Res Notes. 2011 Oct 7;4:386. doi: 10.1186/1756-0500-4-386. BMC Res Notes. 2011. PMID: 21981765 Free PMC article.

7

Evaluating the effective numbers of independent tests and significant p-value thresholds in commercial genotyping arrays and public imputation reference datasets.

Li MX, Yeung JM, Cherny SS, Sham PC. Li MX, et al. Hum Genet. 2012 May;131(5):747-56. doi: 10.1007/s00439-011-1118-2. Epub 2011 Dec 6. Hum Genet. 2012. PMID: 22143225 Free PMC article.

8

A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases.

Li MX, Gui HS, Kwan JS, Bao SY, Sham PC. Li MX, et al. Nucleic Acids Res. 2012 Apr;40(7):e53. doi: 10.1093/nar/gkr1257. Epub 2012 Jan 12. Nucleic Acids Res. 2012. PMID: 22241780 Free PMC article.

9

HYST: a hybrid set-based test for genome-wide association studies, with application to protein-protein interaction-based association analysis.

Li MX, Kwan JS, Sham PC. Li MX, et al. Am J Hum Genet. 2012 Sep 7;91(3):478-88. doi: 10.1016/j.ajhg.2012.08.004. Am J Hum Genet. 2012. PMID: 22958900 Free PMC article.

10

Predicting mendelian disease-causing non-synonymous single nucleotide variants in exome sequencing studies.

Li MX, Kwan JS, Bao SY, Yang W, Ho SL, Song YQ, Sham PC. Li MX, et al. PLoS Genet. 2013;9(1):e1003143. doi: 10.1371/journal.pgen.1003143. Epub 2013 Jan 17. PLoS Genet. 2013. PMID: 23341771 Free PMC article.

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